Tranexamic Acid
- Product NDC
- 17478-018
- 11-digit product format
- 174780018
- Labeler code
- 17478
- Product ID
- 17478-018_c287004b-1794-4c41-ad66-5bdfdd9a219b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Tranexamic Acid
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAVENOUS
- Labeler
- Akorn
- Application
- ANDA206594
- Marketing category
- ANDA
- Marketing start
- 2017-09-28
- Marketing end
- 0000-00-00
- Substance
- TRANEXAMIC ACID
- Active strength
- 100 mg/mL
- Pharmacologic classes
- Antifibrinolytic Agent [EPC], Decreased Fibrinolysis [PE]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 17478-018-10 | 17478001810 | 10 VIAL, SINGLE-DOSE in 1 CARTON (17478-018-10) > 10 mL in 1 VIAL, SINGLE-DOSE | 2017-09-28 | 0000-00-00 | No | No | Current |